TY - JOUR
T1 - Electrically stimulated droplet injector for reduced sample consumption in serial crystallography
AU - Sonker, Mukul
AU - Doppler, Diandra
AU - Egatz-Gomez, Ana
AU - Zaare, Sahba
AU - Rabbani, Mohammad T.
AU - Manna, Abhik
AU - Cruz Villarreal, Jorvani
AU - Nelson, Garrett
AU - Ketawala, Gihan K.
AU - Karpos, Konstantinos
AU - Alvarez, Roberto C.
AU - Nazari, Reza
AU - Thifault, Darren
AU - Jernigan, Rebecca
AU - Oberthür, Dominik
AU - Han, Huijong
AU - Sierra, Raymond
AU - Hunter, Mark S.
AU - Batyuk, Alexander
AU - Kupitz, Christopher J.
AU - Sublett, Robert E.
AU - Poitevin, Frederic
AU - Lisova, Stella
AU - Mariani, Valerio
AU - Tolstikova, Alexandra
AU - Boutet, Sebastien
AU - Messerschmidt, Marc
AU - Meza-Aguilar, J. Domingo
AU - Fromme, Raimund
AU - Martin-Garcia, Jose M.
AU - Botha, Sabine
AU - Fromme, Petra
AU - Grant, Thomas D.
AU - Kirian, Richard A.
AU - Ros, Alexandra
N1 - Publisher Copyright:
© 2022 The Authors
PY - 2022/12/14
Y1 - 2022/12/14
N2 - With advances in X-ray free-electron lasers (XFELs), serial femtosecond crystallography (SFX) has enabled the static and dynamic structure determination for challenging proteins such as membrane protein complexes. In SFX with XFELs, the crystals are typically destroyed after interacting with a single XFEL pulse. Therefore, thousands of new crystals must be sequentially introduced into the X-ray beam to collect full data sets. Because of the serial nature of any SFX experiment, up to 99% of the sample delivered to the X-ray beam during its “off-time” between X-ray pulses is wasted due to the intrinsic pulsed nature of all current XFELs. To solve this major problem of large and often limiting sample consumption, we report on improvements of a revolutionary sample-saving method that is compatible with all current XFELs. We previously reported 3D-printed injection devices coupled with gas dynamic virtual nozzles (GDVNs) capable of generating samples containing droplets segmented by an immiscible oil phase for jetting crystal-laden droplets into the path of an XFEL. Here, we have further improved the device design by including metal electrodes inducing electrowetting effects for improved control over droplet generation frequency to stimulate the droplet release to matching the XFEL repetition rate by employing an electrical feedback mechanism. We report the improvements in this electrically triggered segmented flow approach for sample conservation in comparison with a continuous GDVN injection using the microcrystals of lysozyme and 3-deoxy-D-manno-octulosonate 8-phosphate synthase and report the segmented flow approach for sample injection applied at the Macromolecular Femtosecond Crystallography instrument at the Linear Coherent Light Source for the first time.
AB - With advances in X-ray free-electron lasers (XFELs), serial femtosecond crystallography (SFX) has enabled the static and dynamic structure determination for challenging proteins such as membrane protein complexes. In SFX with XFELs, the crystals are typically destroyed after interacting with a single XFEL pulse. Therefore, thousands of new crystals must be sequentially introduced into the X-ray beam to collect full data sets. Because of the serial nature of any SFX experiment, up to 99% of the sample delivered to the X-ray beam during its “off-time” between X-ray pulses is wasted due to the intrinsic pulsed nature of all current XFELs. To solve this major problem of large and often limiting sample consumption, we report on improvements of a revolutionary sample-saving method that is compatible with all current XFELs. We previously reported 3D-printed injection devices coupled with gas dynamic virtual nozzles (GDVNs) capable of generating samples containing droplets segmented by an immiscible oil phase for jetting crystal-laden droplets into the path of an XFEL. Here, we have further improved the device design by including metal electrodes inducing electrowetting effects for improved control over droplet generation frequency to stimulate the droplet release to matching the XFEL repetition rate by employing an electrical feedback mechanism. We report the improvements in this electrically triggered segmented flow approach for sample conservation in comparison with a continuous GDVN injection using the microcrystals of lysozyme and 3-deoxy-D-manno-octulosonate 8-phosphate synthase and report the segmented flow approach for sample injection applied at the Macromolecular Femtosecond Crystallography instrument at the Linear Coherent Light Source for the first time.
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U2 - 10.1016/j.bpr.2022.100081
DO - 10.1016/j.bpr.2022.100081
M3 - Article
AN - SCOPUS:85140085737
SN - 2667-0747
VL - 2
JO - Biophysical Reports
JF - Biophysical Reports
IS - 4
M1 - 100081
ER -